US20150190664A1 - Fire extinguishing composition containing transition metal compound - Google Patents
Fire extinguishing composition containing transition metal compound Download PDFInfo
- Publication number
- US20150190664A1 US20150190664A1 US14/374,837 US201214374837A US2015190664A1 US 20150190664 A1 US20150190664 A1 US 20150190664A1 US 201214374837 A US201214374837 A US 201214374837A US 2015190664 A1 US2015190664 A1 US 2015190664A1
- Authority
- US
- United States
- Prior art keywords
- fire extinguishing
- salt
- transition metal
- metal compound
- hydrochloride
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 51
- 150000003623 transition metal compounds Chemical class 0.000 title claims abstract description 25
- 150000007524 organic acids Chemical class 0.000 claims abstract description 58
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 44
- -1 amine salt Chemical class 0.000 claims abstract description 33
- 150000003839 salts Chemical class 0.000 claims abstract description 29
- 239000000463 material Substances 0.000 claims abstract description 20
- 239000004615 ingredient Substances 0.000 claims abstract description 11
- 150000001412 amines Chemical class 0.000 claims abstract description 9
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 28
- 229910052723 transition metal Inorganic materials 0.000 claims description 17
- 235000019359 magnesium stearate Nutrition 0.000 claims description 14
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 12
- 150000003624 transition metals Chemical class 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 9
- 230000000996 additive effect Effects 0.000 claims description 9
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 claims description 8
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 7
- UPPLJLAHMKABPR-UHFFFAOYSA-H 2-hydroxypropane-1,2,3-tricarboxylate;nickel(2+) Chemical compound [Ni+2].[Ni+2].[Ni+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O UPPLJLAHMKABPR-UHFFFAOYSA-H 0.000 claims description 6
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims description 6
- 150000001868 cobalt Chemical class 0.000 claims description 6
- 229940011182 cobalt acetate Drugs 0.000 claims description 6
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 claims description 6
- 150000001879 copper Chemical class 0.000 claims description 6
- YEOCHZFPBYUXMC-UHFFFAOYSA-L copper benzoate Chemical compound [Cu+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 YEOCHZFPBYUXMC-UHFFFAOYSA-L 0.000 claims description 6
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims description 6
- RSJOBNMOMQFPKQ-UHFFFAOYSA-L copper;2,3-dihydroxybutanedioate Chemical compound [Cu+2].[O-]C(=O)C(O)C(O)C([O-])=O RSJOBNMOMQFPKQ-UHFFFAOYSA-L 0.000 claims description 6
- VEPSWGHMGZQCIN-UHFFFAOYSA-H ferric oxalate Chemical compound [Fe+3].[Fe+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O VEPSWGHMGZQCIN-UHFFFAOYSA-H 0.000 claims description 6
- 150000002696 manganese Chemical class 0.000 claims description 6
- 150000002815 nickel Chemical class 0.000 claims description 6
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 6
- 150000003751 zinc Chemical class 0.000 claims description 6
- 239000004246 zinc acetate Substances 0.000 claims description 6
- FOUQLSBYBRTDKN-UHFFFAOYSA-L 2-carboxyphenolate;cobalt(2+) Chemical compound [Co+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O FOUQLSBYBRTDKN-UHFFFAOYSA-L 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 5
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 claims description 5
- CBPYOHALYYGNOE-UHFFFAOYSA-M potassium;3,5-dinitrobenzoate Chemical compound [K+].[O-]C(=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 CBPYOHALYYGNOE-UHFFFAOYSA-M 0.000 claims description 5
- 229910021653 sulphate ion Inorganic materials 0.000 claims description 5
- SCNCIXKLOBXDQB-UHFFFAOYSA-K cobalt(3+);2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Co+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O SCNCIXKLOBXDQB-UHFFFAOYSA-K 0.000 claims description 4
- LDXYDHGRKFMULJ-UHFFFAOYSA-N (3-azaniumylphenyl)azanium;sulfate Chemical compound OS(O)(=O)=O.NC1=CC=CC(N)=C1 LDXYDHGRKFMULJ-UHFFFAOYSA-N 0.000 claims description 3
- NEPWWHQLHRGVQL-UHFFFAOYSA-N 1-n,4-n-dimethylbenzene-1,4-diamine;hydron;chloride Chemical compound Cl.CNC1=CC=C(NC)C=C1 NEPWWHQLHRGVQL-UHFFFAOYSA-N 0.000 claims description 3
- BMFMTNROJASFBW-UHFFFAOYSA-N 2-(furan-2-ylmethylsulfinyl)acetic acid Chemical compound OC(=O)CS(=O)CC1=CC=CO1 BMFMTNROJASFBW-UHFFFAOYSA-N 0.000 claims description 3
- BNZCDZDLTIHJAC-UHFFFAOYSA-N 2-azaniumylethylazanium;sulfate Chemical compound NCC[NH3+].OS([O-])(=O)=O BNZCDZDLTIHJAC-UHFFFAOYSA-N 0.000 claims description 3
- UDIKHQMWHQJPNT-UHFFFAOYSA-N 2-bromoaniline;hydrochloride Chemical compound Cl.NC1=CC=CC=C1Br UDIKHQMWHQJPNT-UHFFFAOYSA-N 0.000 claims description 3
- OZIKUNPJXSWSMD-UHFFFAOYSA-L 2-carboxyphenolate;manganese(2+) Chemical compound [Mn+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O OZIKUNPJXSWSMD-UHFFFAOYSA-L 0.000 claims description 3
- DGOFDXKSKYTBGX-UHFFFAOYSA-L 2-carboxyphenolate;nickel(2+) Chemical compound [Ni+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O DGOFDXKSKYTBGX-UHFFFAOYSA-L 0.000 claims description 3
- ZRNHBOAYYNHVOY-UHFFFAOYSA-K 2-hydroxybenzoate;iron(3+) Chemical compound [Fe+3].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O ZRNHBOAYYNHVOY-UHFFFAOYSA-K 0.000 claims description 3
- OAVRWNUUOUXDFH-UHFFFAOYSA-H 2-hydroxypropane-1,2,3-tricarboxylate;manganese(2+) Chemical compound [Mn+2].[Mn+2].[Mn+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O OAVRWNUUOUXDFH-UHFFFAOYSA-H 0.000 claims description 3
- DPJCXCZTLWNFOH-UHFFFAOYSA-N 2-nitroaniline Chemical compound NC1=CC=CC=C1[N+]([O-])=O DPJCXCZTLWNFOH-UHFFFAOYSA-N 0.000 claims description 3
- DCBCSMXGLXAXDM-UHFFFAOYSA-N 3-aminophenol;hydrochloride Chemical compound [Cl-].[NH3+]C1=CC=CC(O)=C1 DCBCSMXGLXAXDM-UHFFFAOYSA-N 0.000 claims description 3
- PACLNJPTGMYEKW-UHFFFAOYSA-N 3-aminophenol;sulfuric acid Chemical compound OS([O-])(=O)=O.[NH3+]C1=CC=CC(O)=C1 PACLNJPTGMYEKW-UHFFFAOYSA-N 0.000 claims description 3
- GJMPSRSMBJLKKB-UHFFFAOYSA-N 3-methylphenylacetic acid Chemical compound CC1=CC=CC(CC(O)=O)=C1 GJMPSRSMBJLKKB-UHFFFAOYSA-N 0.000 claims description 3
- LUKPNZHXJRJBAN-UHFFFAOYSA-N 4-(4-amino-3-methylphenyl)-2-methylaniline;hydron;dichloride Chemical compound [Cl-].[Cl-].C1=C([NH3+])C(C)=CC(C=2C=C(C)C([NH3+])=CC=2)=C1 LUKPNZHXJRJBAN-UHFFFAOYSA-N 0.000 claims description 3
- ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 claims description 3
- HAAZMOAXEMIBAJ-UHFFFAOYSA-N 4-chloro-2-methylquinazoline Chemical compound C1=CC=CC2=NC(C)=NC(Cl)=C21 HAAZMOAXEMIBAJ-UHFFFAOYSA-N 0.000 claims description 3
- IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 claims description 3
- JXSRRBVHLUJJFC-UHFFFAOYSA-N 7-amino-2-methylsulfanyl-[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile Chemical compound N1=CC(C#N)=C(N)N2N=C(SC)N=C21 JXSRRBVHLUJJFC-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- CZNVSLGYWMSMKE-OPDGVEILSA-K Ferric gluconate Chemical compound [Fe+3].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O CZNVSLGYWMSMKE-OPDGVEILSA-K 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 3
- WHMDKBIGKVEYHS-IYEMJOQQSA-L Zinc gluconate Chemical compound [Zn+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O WHMDKBIGKVEYHS-IYEMJOQQSA-L 0.000 claims description 3
- ZOXJIQNURSAHRV-UHFFFAOYSA-N [4-(4-azaniumylphenyl)phenyl]azanium;sulfate Chemical compound [O-]S([O-])(=O)=O.C1=CC([NH3+])=CC=C1C1=CC=C([NH3+])C=C1 ZOXJIQNURSAHRV-UHFFFAOYSA-N 0.000 claims description 3
- MQRWBMAEBQOWAF-UHFFFAOYSA-N acetic acid;nickel Chemical compound [Ni].CC(O)=O.CC(O)=O MQRWBMAEBQOWAF-UHFFFAOYSA-N 0.000 claims description 3
- MMCPOSDMTGQNKG-UJZMCJRSSA-N aniline;hydrochloride Chemical compound Cl.N[14C]1=[14CH][14CH]=[14CH][14CH]=[14CH]1 MMCPOSDMTGQNKG-UJZMCJRSSA-N 0.000 claims description 3
- GNNALEGJVYVIIH-UHFFFAOYSA-N benzene-1,2-diamine;hydrochloride Chemical compound Cl.NC1=CC=CC=C1N GNNALEGJVYVIIH-UHFFFAOYSA-N 0.000 claims description 3
- URGXGBOBXYFSAF-UHFFFAOYSA-N benzene-1,2-diamine;sulfuric acid Chemical compound OS(O)(=O)=O.NC1=CC=CC=C1N URGXGBOBXYFSAF-UHFFFAOYSA-N 0.000 claims description 3
- VEGZHURRCWERMK-UHFFFAOYSA-N benzene-1,3-diamine;hydrochloride Chemical compound Cl.NC1=CC=CC(N)=C1 VEGZHURRCWERMK-UHFFFAOYSA-N 0.000 claims description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- GAYAMOAYBXKUII-UHFFFAOYSA-L cobalt(2+);dibenzoate Chemical compound [Co+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 GAYAMOAYBXKUII-UHFFFAOYSA-L 0.000 claims description 3
- WLQXLCXXAPYDIU-UHFFFAOYSA-L cobalt(2+);disulfamate Chemical compound [Co+2].NS([O-])(=O)=O.NS([O-])(=O)=O WLQXLCXXAPYDIU-UHFFFAOYSA-L 0.000 claims description 3
- MULYSYXKGICWJF-UHFFFAOYSA-L cobalt(2+);oxalate Chemical compound [Co+2].[O-]C(=O)C([O-])=O MULYSYXKGICWJF-UHFFFAOYSA-L 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- CXGHLNDIGXESIH-GRVYQHKQSA-L copper;(9z,12z)-octadeca-9,12-dienoate Chemical compound [Cu+2].CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O.CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O CXGHLNDIGXESIH-GRVYQHKQSA-L 0.000 claims description 3
- SVOAENZIOKPANY-CVBJKYQLSA-L copper;(z)-octadec-9-enoate Chemical compound [Cu+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O SVOAENZIOKPANY-CVBJKYQLSA-L 0.000 claims description 3
- CMRVDFLZXRTMTH-UHFFFAOYSA-L copper;2-carboxyphenolate Chemical compound [Cu+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O CMRVDFLZXRTMTH-UHFFFAOYSA-L 0.000 claims description 3
- ZKHSDHFSDPLKDI-UHFFFAOYSA-L copper;2-hydroxybutanedioate Chemical compound [Cu+2].[O-]C(=O)C(O)CC([O-])=O ZKHSDHFSDPLKDI-UHFFFAOYSA-L 0.000 claims description 3
- HFDWIMBEIXDNQS-UHFFFAOYSA-L copper;diformate Chemical compound [Cu+2].[O-]C=O.[O-]C=O HFDWIMBEIXDNQS-UHFFFAOYSA-L 0.000 claims description 3
- QYCVHILLJSYYBD-UHFFFAOYSA-L copper;oxalate Chemical compound [Cu+2].[O-]C(=O)C([O-])=O QYCVHILLJSYYBD-UHFFFAOYSA-L 0.000 claims description 3
- FWBOFUGDKHMVPI-UHFFFAOYSA-K dicopper;2-oxidopropane-1,2,3-tricarboxylate Chemical compound [Cu+2].[Cu+2].[O-]C(=O)CC([O-])(C([O-])=O)CC([O-])=O FWBOFUGDKHMVPI-UHFFFAOYSA-K 0.000 claims description 3
- NLXFONFHPKEHOZ-UHFFFAOYSA-N diethylazanium;hydron;sulfate Chemical compound CCNCC.OS(O)(=O)=O NLXFONFHPKEHOZ-UHFFFAOYSA-N 0.000 claims description 3
- XHFGWHUWQXTGAT-UHFFFAOYSA-N dimethylamine hydrochloride Natural products CNC(C)C XHFGWHUWQXTGAT-UHFFFAOYSA-N 0.000 claims description 3
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 claims description 3
- HCFPRFJJTHMING-UHFFFAOYSA-N ethane-1,2-diamine;hydron;chloride Chemical compound [Cl-].NCC[NH3+] HCFPRFJJTHMING-UHFFFAOYSA-N 0.000 claims description 3
- MFGZXPGKKJMZIY-UHFFFAOYSA-N ethyl 5-amino-1-(4-sulfamoylphenyl)pyrazole-4-carboxylate Chemical compound NC1=C(C(=O)OCC)C=NN1C1=CC=C(S(N)(=O)=O)C=C1 MFGZXPGKKJMZIY-UHFFFAOYSA-N 0.000 claims description 3
- 229960002413 ferric citrate Drugs 0.000 claims description 3
- OGVXWEOZQMAAIM-UHFFFAOYSA-N hydron;2-methylaniline;chloride Chemical compound Cl.CC1=CC=CC=C1N OGVXWEOZQMAAIM-UHFFFAOYSA-N 0.000 claims description 3
- JEFJSEIUEJBMSR-UHFFFAOYSA-N hydron;n-phenylaniline;chloride Chemical compound Cl.C=1C=CC=CC=1NC1=CC=CC=C1 JEFJSEIUEJBMSR-UHFFFAOYSA-N 0.000 claims description 3
- 229910000378 hydroxylammonium sulfate Inorganic materials 0.000 claims description 3
- AEJDTAYHARDWRW-VLKMOBIUSA-K iron(3+);(9z,12z)-octadeca-9,12-dienoate Chemical compound [Fe+3].CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O.CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O.CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O AEJDTAYHARDWRW-VLKMOBIUSA-K 0.000 claims description 3
- HOIQWTMREPWSJY-GNOQXXQHSA-K iron(3+);(z)-octadec-9-enoate Chemical compound [Fe+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O HOIQWTMREPWSJY-GNOQXXQHSA-K 0.000 claims description 3
- XHQSLVIGPHXVAK-UHFFFAOYSA-K iron(3+);octadecanoate Chemical compound [Fe+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XHQSLVIGPHXVAK-UHFFFAOYSA-K 0.000 claims description 3
- PVFSDGKDKFSOTB-UHFFFAOYSA-K iron(3+);triacetate Chemical compound [Fe+3].CC([O-])=O.CC([O-])=O.CC([O-])=O PVFSDGKDKFSOTB-UHFFFAOYSA-K 0.000 claims description 3
- ITAUHKJMPRCVIH-UHFFFAOYSA-K iron(3+);tribenzoate Chemical compound [Fe+3].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 ITAUHKJMPRCVIH-UHFFFAOYSA-K 0.000 claims description 3
- NPFOYSMITVOQOS-UHFFFAOYSA-K iron(III) citrate Chemical compound [Fe+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NPFOYSMITVOQOS-UHFFFAOYSA-K 0.000 claims description 3
- 239000011564 manganese citrate Substances 0.000 claims description 3
- 235000014872 manganese citrate Nutrition 0.000 claims description 3
- 229940097206 manganese citrate Drugs 0.000 claims description 3
- 239000011683 manganese gluconate Substances 0.000 claims description 3
- 235000014012 manganese gluconate Nutrition 0.000 claims description 3
- 229940072543 manganese gluconate Drugs 0.000 claims description 3
- OXHQNTSSPHKCPB-IYEMJOQQSA-L manganese(2+);(2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanoate Chemical compound [Mn+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OXHQNTSSPHKCPB-IYEMJOQQSA-L 0.000 claims description 3
- RGVLTEMOWXGQOS-UHFFFAOYSA-L manganese(2+);oxalate Chemical compound [Mn+2].[O-]C(=O)C([O-])=O RGVLTEMOWXGQOS-UHFFFAOYSA-L 0.000 claims description 3
- BVSPUXSSEOUOMK-UHFFFAOYSA-N n-(hydroxymethyl)benzenesulfonamide Chemical compound OCNS(=O)(=O)C1=CC=CC=C1 BVSPUXSSEOUOMK-UHFFFAOYSA-N 0.000 claims description 3
- FOKKJVHTXPJHEN-UHFFFAOYSA-N naphthalen-1-ylazanium;chloride Chemical compound Cl.C1=CC=C2C(N)=CC=CC2=C1 FOKKJVHTXPJHEN-UHFFFAOYSA-N 0.000 claims description 3
- 229940078494 nickel acetate Drugs 0.000 claims description 3
- LVBIMKHYBUACBU-CVBJKYQLSA-L nickel(2+);(z)-octadec-9-enoate Chemical compound [Ni+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LVBIMKHYBUACBU-CVBJKYQLSA-L 0.000 claims description 3
- GAIQJSWQJOZOMI-UHFFFAOYSA-L nickel(2+);dibenzoate Chemical compound [Ni+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 GAIQJSWQJOZOMI-UHFFFAOYSA-L 0.000 claims description 3
- KERTUBUCQCSNJU-UHFFFAOYSA-L nickel(2+);disulfamate Chemical compound [Ni+2].NS([O-])(=O)=O.NS([O-])(=O)=O KERTUBUCQCSNJU-UHFFFAOYSA-L 0.000 claims description 3
- DOLZKNFSRCEOFV-UHFFFAOYSA-L nickel(2+);oxalate Chemical compound [Ni+2].[O-]C(=O)C([O-])=O DOLZKNFSRCEOFV-UHFFFAOYSA-L 0.000 claims description 3
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 3
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 claims description 3
- 229950000975 salicylanilide Drugs 0.000 claims description 3
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 claims description 3
- 229940117957 triethanolamine hydrochloride Drugs 0.000 claims description 3
- WGIWBXUNRXCYRA-UHFFFAOYSA-H trizinc;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WGIWBXUNRXCYRA-UHFFFAOYSA-H 0.000 claims description 3
- 239000011746 zinc citrate Substances 0.000 claims description 3
- 235000006076 zinc citrate Nutrition 0.000 claims description 3
- 229940068475 zinc citrate Drugs 0.000 claims description 3
- 239000011670 zinc gluconate Substances 0.000 claims description 3
- 235000011478 zinc gluconate Nutrition 0.000 claims description 3
- 229960000306 zinc gluconate Drugs 0.000 claims description 3
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 3
- 229940057977 zinc stearate Drugs 0.000 claims description 3
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 claims description 3
- JDLYKQWJXAQNNS-UHFFFAOYSA-L zinc;dibenzoate Chemical compound [Zn+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 JDLYKQWJXAQNNS-UHFFFAOYSA-L 0.000 claims description 3
- ZPEJZWGMHAKWNL-UHFFFAOYSA-L zinc;oxalate Chemical compound [Zn+2].[O-]C(=O)C([O-])=O ZPEJZWGMHAKWNL-UHFFFAOYSA-L 0.000 claims description 3
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical group OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 235000012222 talc Nutrition 0.000 claims description 2
- ZEMODTUZIWTRPF-UHFFFAOYSA-N 1-n,4-n-diethylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(NCC)C=C1 ZEMODTUZIWTRPF-UHFFFAOYSA-N 0.000 claims 1
- NULAJYZBOLVQPQ-UHFFFAOYSA-N N-(1-naphthyl)ethylenediamine Chemical compound C1=CC=C2C(NCCN)=CC=CC2=C1 NULAJYZBOLVQPQ-UHFFFAOYSA-N 0.000 claims 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 239000000443 aerosol Substances 0.000 abstract description 27
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 238000002347 injection Methods 0.000 abstract 1
- 239000007924 injection Substances 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 35
- 239000001913 cellulose Substances 0.000 description 13
- 229920002678 cellulose Polymers 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 238000003825 pressing Methods 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 239000007789 gas Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 5
- 229940071125 manganese acetate Drugs 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 238000002485 combustion reaction Methods 0.000 description 4
- 239000002826 coolant Substances 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- AKVAGWOVWQDTAF-UHFFFAOYSA-N 1-bromo-4-(1-isocyanatoethyl)benzene Chemical compound O=C=NC(C)C1=CC=C(Br)C=C1 AKVAGWOVWQDTAF-UHFFFAOYSA-N 0.000 description 2
- HRBLHUVHOWWBEN-UHFFFAOYSA-N 1-n,4-n-diethylbenzene-1,4-diamine;hydrochloride Chemical compound Cl.CCNC1=CC=C(NCC)C=C1 HRBLHUVHOWWBEN-UHFFFAOYSA-N 0.000 description 2
- 229920004449 Halon® Polymers 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- NZTCRHBIQWZHEY-UHFFFAOYSA-N (4-azaniumylphenyl)-methylazanium;sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(N)C=C1 NZTCRHBIQWZHEY-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229940076286 cupric acetate Drugs 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- WZRRZVUZWWMSKH-UHFFFAOYSA-N n'-naphthalen-1-ylethane-1,2-diamine;hydrochloride Chemical compound Cl.C1=CC=C2C(NCCN)=CC=CC2=C1 WZRRZVUZWWMSKH-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/06—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires containing gas-producing, chemically-reactive components
Definitions
- the disclosure relates to the technical field of fire prevention and extinguishment, and more particularly to an aerosol fire extinguishing agent containing a transition metal compound.
- Aerosol fire extinguishing agent which is a novel non-toxic harmless fire extinguishing agent with high fire extinguishing efficiency, zero Ozone Depletion Potential (ODP), extremely low residues and little equipment investment, is strongly supported by the government and meets market demands under the urgent background of Halon elimination. Therefore, aerosol fire extinguishing technology has become one of the noticeable alternative technologies of Halon in the past dozen years.
- ODP Ozone Depletion Potential
- Major fire extinguishing mechanisms of aerosol generator are as follows: 1. heat absorption and cooling; 2. chemical inhibition; 3. smothering; 4. isolation; chemical inhibition is the primary mechanism.
- the aerosol generator is obviously advantageous in aspects including fire extinguishing efficiency, storage conditions, engineering cost, maintenance management, toxicity, secondary damage, environment protection and fire extinguishing concentration etc. Oxidation-reduction reactions of the aerosol generator releases a great quantity of gas and active particles while releasing a great deal of heat to bring disadvantages in usage.
- a cooling system of a fire extinguishing apparatus needs to be improved in order to cool the equipment and the aerosol to avoid a secondary fire. Conventional physical cooling results in a complex and heavy equipment structure, complicated processes and high cost.
- the disclosure provides a fire extinguishing composition containing a transition metal compound.
- a fire extinguishing composition containing a transition metal compound, including a salt of an organic acid of the fourth period elements of transition metals in a subgroup and the group VIII; and the fire extinguishing composition adopts a pyrotechnic agent as a heat source and a power source, reacts and releases a fire extinguishing material through heat emitted by igniting and burning the pyrotechnic agent.
- the mass percentage of the salt of the organic acid is 65 wt % to 95 wt %.
- the salt of the organic acid of the fourth period transition metals in the subgroup is a salt of an organic acid of a transition metal element in the group IB, the group IIB or the group VIIB.
- the salt of the organic acid of the fourth period transition metals in the subgroup and group VIII is a ferric salt of an organic acid, a manganese salt of an organic acid, a nickel salt of an organic acid, a copper salt of an organic acid, a zinc salt of an organic acid or a cobalt salt of an organic acid.
- ferric salt of the organic acid is one or more of ferric citrate, ferric oxalate, ferric oleate, ferric linoleate, ferric stearate, ferric benzoate, ferric acetate, ferric salicylate and ferric gluconate.
- the manganese salt of the organic acid is one or more of manganous acetate, manganese oxalate, manganese citrate, manganous benzoate, manganese salicylate and manganese gluconate.
- the nickel salt of the organic acid is one or more of nickel acetate, nickel oxalate, nickel oleate, nickel citrate, nickel benzoate, nickel salicylate and nickel aminosulfonate.
- the copper salt of the organic acid is one or more of copper acetate, copper formate, copper oxalate, copper oleate, copper linoleate, copper stearate, copper citrate, copper tartrate, copper 2-hydroxybutanedioate, copper iso-octoate, copper benzoate, and copper salicylate.
- the zinc salt of the organic acid is one or more of zinc acetate, zinc oxalate, zinc oleate, zinc stearate, zinc citrate, zinc benzoate, zinc methacrylate, zinc salicylate and zinc gluconate.
- the cobalt salt of the organic acid is one or more of cobalt acetate, cobalt oxalate, cobalt citrate, cobalt citrate, cobalt iso-octoate, cobalt benzoate, cobalt salicylate and cobalt amino-sulfonate.
- the fire extinguishing composition further includes an auxiliary fire extinguishing agent in a mass percentage of 5 wt % to 35 wt %.
- auxiliary fire extinguishing agent is an amine and/or organic amine salt.
- the organic amine salt includes an organic amine hydrochloride and an organic amine sulfate.
- the organic amine hydrochloride is one or more of 2-methylaniline hydrochloride, 3,3′-dimethylbenzidine dihydrochloride, N′N-di methyl-p-phenylenediamine sulphate, N,N′-dimethyl-p-phenylenediamine monohydrochloride, N′N-diethyl-p-phenylenediamine sulphate, N,N′-diethyl-p-phenylenediamine monohydrochloride, 1-naphthylamine hydrochloride, aniline hydrochloride, 3-hydroxyphenylamine hydrochloride, diphenylamine hydrochloride, dimethylamine hydrochloride, diethylamine hydrochloride, cyclohexylamine hydrochloride, benzidine sulfate, benzidine hydrochloride, trimethylamine hydrochlorate, triethylamine hydrochlorate, ethylenediamine hydrochloride, m-phenyl
- the organic amine sulfate is one or more of m-phenylenediamine sulfate, hydroxylamine sulfate, o-phenylenediamine sulfate, 3-hydroxyphenylamine sulfate, ethylenediamine sulfate and diethylamine sulfate.
- the amine is one or more of o-nitroaniline, methacrylamide, salicylanilide, p-toluenesulfonamide, p-phenetidine, N-hydroxymethyl benzene sulfonamide, phthalimide and N,N′-methylenebisacrylamide.
- the fire extinguishing composition of the disclosure further includes a performance additive; the performance additive is hydroxy propyl methyl cellulose, magnesium stearate, talc or a combination thereof; the mass percentage of the performance additive ranging from not larger than 0 to smaller than or equal to 15%.
- the salt of the organic acid of the fourth period transition metals 75 wt % to 90 wt %;
- auxiliary fire extinguishing agent 5 wt % to 20 wt %;
- the fire extinguishing mechanism of the fire extinguishing composition of the disclosure is as follows:
- the salt of the organic acid of the transition metal in the fire extinguishing composition of the disclosure can decompose at high temperature to release active metal particle which can react with O., OH., H. free radicals generated by combustion reaction, so as to cut off the combustion reaction chain; at the same time, the fire is extinguished jointly by the physical cooling effect of aerosol grains and the chemical inhibitory effect of the aerosol itself; at the same time, the auxiliary fire extinguishing agent can release a large quantity of gas to increase the gas pressure of the aerosol, the gas is generally N 2 and CO 2 ; these gases can smother flames, have synergistic effect with the pyrotechnic agent and be together sprayed rapidly to reach the fire source to extinguish the fire, thus further improving the fire extinguishing efficacy of the fire extinguishing agent and greatly shortening the effective fire extinguishing time.
- the disclosure uses the salt of the organic acid of the fourth period elements in the subgroup and the group VIII; since the transition metal element shows higher activity, more easily captures free radicals in combustion reaction, cuts off the reaction chain rapidly, realizes a better fire extinguishing effect; a great quantity of fire extinguishing material is generated by heating and decomposing the transition metal element to absorb heat to reduce the equipment temperature and the temperature of a generated aerosol on one hand, and to be sprayed with an aerosol generator, i.e. a pyrotechnic agent, to extinguish a fire on the other hand;
- an aerosol generator i.e. a pyrotechnic agent
- the amine and/or the organic amine salt of the disclosure are/is heated to decompose to generate a large quantity of N 2 and CO 2 gases, which can regulate the concentration and pressure intensity of the fire extinguishing aerosol and improve the spraying intensity of the fire extinguishing material; at the same time, the N 2 and CO 2 gases can extinguish the fire through smothering, and act with the salt of the organic acid of the transition metal to greatly improve the fire extinguishing efficacy of the fire extinguishing composition;
- the proportions of fire extinguishing composition of the disclosure is optimize, the ingredients are fully reacted to avoid residues from blocking a nozzle of the fire extinguishing apparatus, and each ingredient is effectively utilized, thus, the effective utilization of the fire extinguishing composition is greatly improved;
- the salts of the organic acids of the transition metal applied by the disclosure is stable in chemical properties, not easy to volatilize, can hardly react with each other and can be stored for a long period of time.
- a fire extinguishing composition of the disclosure will be further described in combination with specific examples below:
- the fire extinguishing composition includes a salt of an organic acid of the fourth period transition metal elements in a subgroup and the group VIII, adopts a pyrotechnic agent as a heat source and a power source, reacts and releases a fire extinguishing material in use of heat emitted by igniting and burning the pyrotechnic agent.
- the salt of the organic acid in the subgroup mainly involves a salt of an organic acid of a transition metal element in the group IB, the group IIB or the group VIIB.
- the salt of the organic acid of the fourth period transition metal elements in the subgroup and the group VIII mainly includes one or more of a ferric salt of an organic acid, a manganese salt of an organic acid, a nickel salt of an organic acid, a copper salt of an organic acid, a zinc salt of an organic acid and a cobalt salt of an organic acid.
- the ferric salt of the organic acid is ferric citrate, ferric oxalate, ferric oleate, ferric linoleate, ferric stearate, ferric benzoate, ferric acetate, ferric salicylate or ferric gluconate etc.;
- the manganese salt of the organic acid is manganous acetate, manganese oxalate, manganese citrate, manganous benzoate, manganese salicylate or manganese gluconate etc.
- the nickel salt of the organic acid is nickel acetate, nickel oxalate, nickel oleate, nickel citrate, nickel benzoate, nickel salicylate or nickel aminosulfonate etc.
- the copper salt of the organic acid is copper acetate, copper formate, copper oxalate, copper oleate, copper linoleate, copper stearate, copper citrate, copper tartrate, copper 2-hydroxybutanedioate, copper iso-octoate, copper be
- An auxiliary fire extinguishing agent may be further added, i.e. an amine and/or organic amine salt.
- the organic amine salt includes an organic amine hydrochloride and an organic amine sulfate;
- the organic amine hydrochloride may be one or more of 2-methylaniline hydrochloride, 3,3′-dimethylbenzidine dihydrochloride, N′N-dimethyl-p-phenylenediamine sulphate, N,N′-dimethyl-p-phenylenediamine monohydrochloride, N′N-diethyl-p-phenylenediamine sulphate, N,N′-diethyl-p-phenylenediamine monohydrochloride, 1-naphthylamine hydrochloride, aniline hydrochloride, 3-hydroxyphenylamine hydrochloride, diphenylamine hydrochloride, dimethylamine hydrochloride, diethylamine hydrochloride, cyclohexy
- the organic amine sulfate may be one or more of m-phenylenediamine sulfate, hydroxylamine sulfate, o-phenylenediamine sulfate, 3-hydroxyphenylamine sulfate, ethylenediamine sulfate and diethylamine sulfate.
- the amine may be one or more of o-nitroaniline, methacrylamide, salicylanilide, p-toluenesulfonamide, p-phenetidine, N-hydroxymethylbenzene sulfonamide, phthalimide and N,N′-methylenebisacrylamide.
- a performance additive and an adhesive may be further added, and prepared according to specific ingredients.
- the major difference from the first example is that 65 wt % of cobalt salicylate and 20 wt % of cobalt acetate were used and diethylamine hydrochloride in a mass percentage of 10% was used as an auxiliary fire extinguishing agent; other adhesive, release agent, content thereof and composition preparation etc. were the same as the first example.
- the fire extinguishing compositions were loaded to a fire extinguishing apparatus containing 50 g of a K-type aerosol generator, and 8B fire extinguishing tests were carried out on 3 fires in each group; specific test methods, test models and evaluation methods are as follows, and results are recorded in Table 1:
- test model the oil disk is a GA86-2009 8B circular disk (diameter 570 mm, internal depth 150 mm and approximate area 0.25 m 2 );
- test method 500 mm of water was added to the oil disk, then 2 mm of 93190 gasoline was added, the oil disk was pre-burning for 1 min and then began fire extinguishment;
- a fire extinguishing test was performed for a fire extinguishing apparatus sample containing 100 g of a commercially available K-type hot aerosol fire extinguishing agent according to the same experiment model and experiment method as those in the examples above, and test results are as shown in Table 1.
- test results are as shown in Table 2 of test records.
- test results are as shown in Table 2 of test records.
- test results are as shown in Table 2 of test records.
- test results are as shown in Table 2 of test records.
- test results are as shown in Table 2 of test records.
- test results are as shown in Table 2 of test records.
- test results are as shown in Table 2 of test records.
- a 93# gasoline fire extinguishing test was performed on an oil disk having an area of 0.25 m 2 for a fire extinguishing apparatus sample containing 100 g of a commercially available K-type hot aerosol fire extinguishing agent, and test results are as shown in Table 2.
- the fire extinguishing compositions containing an organic salt of transition metals in the group IB, the group IIB, and the group VIIB can completely meet basic fire extinguishing requirements of national standard GA86-2009 and there are no naked flames at all nozzles; the fire extinguishing performance is obviously better than that of the second comparison example and the fire extinguishing time is short.
- the fire extinguishing compositions containing an organic salt compound of transition metals in the group IB, the group IIB, and the group VIIB can meet ideal fire extinguishing requirements without addition of an auxiliary fire extinguishing ingredient in a certain mass percentage. However, by comprehensively considering aspects including spraying time, fire extinguishing time, the size of nozzle gas flows, spraying stability and processing etc.; a certain amount of an auxiliary fire extinguishing ingredient is added optimally.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Emergency Management (AREA)
- Fire-Extinguishing Compositions (AREA)
Abstract
Description
- The disclosure relates to the technical field of fire prevention and extinguishment, and more particularly to an aerosol fire extinguishing agent containing a transition metal compound.
- Aerosol fire extinguishing agent, which is a novel non-toxic harmless fire extinguishing agent with high fire extinguishing efficiency, zero Ozone Depletion Potential (ODP), extremely low residues and little equipment investment, is strongly supported by the government and meets market demands under the urgent background of Halon elimination. Therefore, aerosol fire extinguishing technology has become one of the noticeable alternative technologies of Halon in the past dozen years.
- Major fire extinguishing mechanisms of aerosol generator are as follows: 1. heat absorption and cooling; 2. chemical inhibition; 3. smothering; 4. isolation; chemical inhibition is the primary mechanism. Although the aerosol generator is obviously advantageous in aspects including fire extinguishing efficiency, storage conditions, engineering cost, maintenance management, toxicity, secondary damage, environment protection and fire extinguishing concentration etc. Oxidation-reduction reactions of the aerosol generator releases a great quantity of gas and active particles while releasing a great deal of heat to bring disadvantages in usage. A cooling system of a fire extinguishing apparatus needs to be improved in order to cool the equipment and the aerosol to avoid a secondary fire. Conventional physical cooling results in a complex and heavy equipment structure, complicated processes and high cost. Physical cooling deactivates a great quantity of active particles, thus greatly reducing the fire extinguishing performance. In addition, the fire extinguishing efficiency is limited, thus causing waste of agent cost to a certain extent. If a chemical cooling method is applied, a coolant is generally placed in a spraying direction of a pyrotechnic fire extinguishing agent. However, a common chemical coolant will affect the fire extinguishing efficiency of the pyrotechnic fire extinguishing agent. Currently, selection of the fire extinguishing composition are still being studied and researched constantly, and the fire extinguishing efficiency of a commercial fire extinguishing agent is not ideal. The stability and spraying intensity of the fire extinguishing composition, considered as a whole, should realize inhibition of flames and rapid and effective inhibition of a fire source.
- In order to overcome disadvantages still existing in the fire extinguishing efficiency and chemical stability of a fire extinguishing composition in the prior art, the disclosure provides a fire extinguishing composition containing a transition metal compound.
- The technical solution to solve the technical problem is as follows:
- a fire extinguishing composition containing a transition metal compound, including a salt of an organic acid of the fourth period elements of transition metals in a subgroup and the group VIII; and the fire extinguishing composition adopts a pyrotechnic agent as a heat source and a power source, reacts and releases a fire extinguishing material through heat emitted by igniting and burning the pyrotechnic agent.
- Further, the mass percentage of the salt of the organic acid is 65 wt % to 95 wt %.
- Further, the salt of the organic acid of the fourth period transition metals in the subgroup is a salt of an organic acid of a transition metal element in the group IB, the group IIB or the group VIIB.
- Further, the salt of the organic acid of the fourth period transition metals in the subgroup and group VIII is a ferric salt of an organic acid, a manganese salt of an organic acid, a nickel salt of an organic acid, a copper salt of an organic acid, a zinc salt of an organic acid or a cobalt salt of an organic acid.
- Further, the ferric salt of the organic acid is one or more of ferric citrate, ferric oxalate, ferric oleate, ferric linoleate, ferric stearate, ferric benzoate, ferric acetate, ferric salicylate and ferric gluconate.
- Further, the manganese salt of the organic acid is one or more of manganous acetate, manganese oxalate, manganese citrate, manganous benzoate, manganese salicylate and manganese gluconate.
- Further, the nickel salt of the organic acid is one or more of nickel acetate, nickel oxalate, nickel oleate, nickel citrate, nickel benzoate, nickel salicylate and nickel aminosulfonate.
- Further, the copper salt of the organic acid is one or more of copper acetate, copper formate, copper oxalate, copper oleate, copper linoleate, copper stearate, copper citrate, copper tartrate, copper 2-hydroxybutanedioate, copper iso-octoate, copper benzoate, and copper salicylate.
- Further, the zinc salt of the organic acid is one or more of zinc acetate, zinc oxalate, zinc oleate, zinc stearate, zinc citrate, zinc benzoate, zinc methacrylate, zinc salicylate and zinc gluconate.
- Further, the cobalt salt of the organic acid is one or more of cobalt acetate, cobalt oxalate, cobalt citrate, cobalt citrate, cobalt iso-octoate, cobalt benzoate, cobalt salicylate and cobalt amino-sulfonate.
- Further, the fire extinguishing composition further includes an auxiliary fire extinguishing agent in a mass percentage of 5 wt % to 35 wt %.
- Further, the auxiliary fire extinguishing agent is an amine and/or organic amine salt.
- Further, the organic amine salt includes an organic amine hydrochloride and an organic amine sulfate.
- Further, the organic amine hydrochloride is one or more of 2-methylaniline hydrochloride, 3,3′-dimethylbenzidine dihydrochloride, N′N-di methyl-p-phenylenediamine sulphate, N,N′-dimethyl-p-phenylenediamine monohydrochloride, N′N-diethyl-p-phenylenediamine sulphate, N,N′-diethyl-p-phenylenediamine monohydrochloride, 1-naphthylamine hydrochloride, aniline hydrochloride, 3-hydroxyphenylamine hydrochloride, diphenylamine hydrochloride, dimethylamine hydrochloride, diethylamine hydrochloride, cyclohexylamine hydrochloride, benzidine sulfate, benzidine hydrochloride, trimethylamine hydrochlorate, triethylamine hydrochlorate, ethylenediamine hydrochloride, m-phenylenediamine hydrochloride, o-phenylendiamine hydrochloride, o-bromoaniline hydrochloride, N-(1-naphthyl)ethylenediamine hydrochloride and triethanolamine hydrochloride.
- Further, the organic amine sulfate is one or more of m-phenylenediamine sulfate, hydroxylamine sulfate, o-phenylenediamine sulfate, 3-hydroxyphenylamine sulfate, ethylenediamine sulfate and diethylamine sulfate.
- Further, the amine is one or more of o-nitroaniline, methacrylamide, salicylanilide, p-toluenesulfonamide, p-phenetidine, N-hydroxymethyl benzene sulfonamide, phthalimide and N,N′-methylenebisacrylamide.
- The fire extinguishing composition of the disclosure further includes a performance additive; the performance additive is hydroxy propyl methyl cellulose, magnesium stearate, talc or a combination thereof; the mass percentage of the performance additive ranging from not larger than 0 to smaller than or equal to 15%.
- Further, in the fire extinguishing composition:
- the salt of the organic acid of the fourth period transition metals: 75 wt % to 90 wt %;
- auxiliary fire extinguishing agent: 5 wt % to 20 wt %;
- performance additive: 5 wt %.
- The fire extinguishing mechanism of the fire extinguishing composition of the disclosure is as follows:
- the salt of the organic acid of the transition metal in the fire extinguishing composition of the disclosure can decompose at high temperature to release active metal particle which can react with O., OH., H. free radicals generated by combustion reaction, so as to cut off the combustion reaction chain; at the same time, the fire is extinguished jointly by the physical cooling effect of aerosol grains and the chemical inhibitory effect of the aerosol itself; at the same time, the auxiliary fire extinguishing agent can release a large quantity of gas to increase the gas pressure of the aerosol, the gas is generally N2 and CO2; these gases can smother flames, have synergistic effect with the pyrotechnic agent and be together sprayed rapidly to reach the fire source to extinguish the fire, thus further improving the fire extinguishing efficacy of the fire extinguishing agent and greatly shortening the effective fire extinguishing time.
- The fire extinguishing composition containing transition metal compound of the disclosure mainly has the following beneficial effect:
- 1. the disclosure uses the salt of the organic acid of the fourth period elements in the subgroup and the group VIII; since the transition metal element shows higher activity, more easily captures free radicals in combustion reaction, cuts off the reaction chain rapidly, realizes a better fire extinguishing effect; a great quantity of fire extinguishing material is generated by heating and decomposing the transition metal element to absorb heat to reduce the equipment temperature and the temperature of a generated aerosol on one hand, and to be sprayed with an aerosol generator, i.e. a pyrotechnic agent, to extinguish a fire on the other hand;
- 2. the amine and/or the organic amine salt of the disclosure are/is heated to decompose to generate a large quantity of N2 and CO2 gases, which can regulate the concentration and pressure intensity of the fire extinguishing aerosol and improve the spraying intensity of the fire extinguishing material; at the same time, the N2 and CO2 gases can extinguish the fire through smothering, and act with the salt of the organic acid of the transition metal to greatly improve the fire extinguishing efficacy of the fire extinguishing composition;
- 3. the proportions of fire extinguishing composition of the disclosure is optimize, the ingredients are fully reacted to avoid residues from blocking a nozzle of the fire extinguishing apparatus, and each ingredient is effectively utilized, thus, the effective utilization of the fire extinguishing composition is greatly improved;
- 4. the salts of the organic acids of the transition metal applied by the disclosure is stable in chemical properties, not easy to volatilize, can hardly react with each other and can be stored for a long period of time.
- A fire extinguishing composition of the disclosure will be further described in combination with specific examples below:
- the fire extinguishing composition includes a salt of an organic acid of the fourth period transition metal elements in a subgroup and the group VIII, adopts a pyrotechnic agent as a heat source and a power source, reacts and releases a fire extinguishing material in use of heat emitted by igniting and burning the pyrotechnic agent. Wherein the salt of the organic acid in the subgroup mainly involves a salt of an organic acid of a transition metal element in the group IB, the group IIB or the group VIIB. The salt of the organic acid of the fourth period transition metal elements in the subgroup and the group VIII mainly includes one or more of a ferric salt of an organic acid, a manganese salt of an organic acid, a nickel salt of an organic acid, a copper salt of an organic acid, a zinc salt of an organic acid and a cobalt salt of an organic acid. The ferric salt of the organic acid is ferric citrate, ferric oxalate, ferric oleate, ferric linoleate, ferric stearate, ferric benzoate, ferric acetate, ferric salicylate or ferric gluconate etc.; the manganese salt of the organic acid is manganous acetate, manganese oxalate, manganese citrate, manganous benzoate, manganese salicylate or manganese gluconate etc.; the nickel salt of the organic acid is nickel acetate, nickel oxalate, nickel oleate, nickel citrate, nickel benzoate, nickel salicylate or nickel aminosulfonate etc.; the copper salt of the organic acid is copper acetate, copper formate, copper oxalate, copper oleate, copper linoleate, copper stearate, copper citrate, copper tartrate, copper 2-hydroxybutanedioate, copper iso-octoate, copper benzoate, or copper salicylate etc.; the zinc salt of the organic acid is zinc acetate, zinc oxalate, zinc oleate, zinc stearate, zinc citrate, zinc benzoate, zinc methacrylate, zinc salicylate or zinc gluconate etc.; the cobalt salt of the organic acid is cobalt acetate, cobalt oxalate, cobalt citrate, cobalt iso-octoate, cobalt benzoate, cobalt salicylate or cobalt amino-sulfonate etc.
- An auxiliary fire extinguishing agent may be further added, i.e. an amine and/or organic amine salt. Wherein the organic amine salt includes an organic amine hydrochloride and an organic amine sulfate; the organic amine hydrochloride may be one or more of 2-methylaniline hydrochloride, 3,3′-dimethylbenzidine dihydrochloride, N′N-dimethyl-p-phenylenediamine sulphate, N,N′-dimethyl-p-phenylenediamine monohydrochloride, N′N-diethyl-p-phenylenediamine sulphate, N,N′-diethyl-p-phenylenediamine monohydrochloride, 1-naphthylamine hydrochloride, aniline hydrochloride, 3-hydroxyphenylamine hydrochloride, diphenylamine hydrochloride, dimethylamine hydrochloride, diethylamine hydrochloride, cyclohexylamine hydrochloride, benzidine sulfate, benzidine hydrochloride, trimethylamine hydrochlorate, triethylamine hydrochlorate, ethylenediamine hydrochloride, m-phenylenediamine hydrochloride, o-phenylendiamine hydrochloride, o-bromoaniline hydrochloride, N-(1-naphthylethyl)enediamine hydrochloride and triethanolamine hydrochloride. The organic amine sulfate may be one or more of m-phenylenediamine sulfate, hydroxylamine sulfate, o-phenylenediamine sulfate, 3-hydroxyphenylamine sulfate, ethylenediamine sulfate and diethylamine sulfate. The amine may be one or more of o-nitroaniline, methacrylamide, salicylanilide, p-toluenesulfonamide, p-phenetidine, N-hydroxymethylbenzene sulfonamide, phthalimide and N,N′-methylenebisacrylamide.
- In order to facilitate processing or production, a performance additive and an adhesive may be further added, and prepared according to specific ingredients.
- The materials above were used for preparing fire extinguishing compositions and tests were carried out, and fire extinguishing experiments were carried out together with a commercially available K-type aerosol fire extinguishing agent in the same conditions, specifically as follows:
- In the present example, 75 wt % of ferric oxalate and 20 wt % of diethylamine hydrochloride were applied as a coolant, 2.5 wt % of hydroxy methyl propyl cellulose was added as an adhesive, industrial alcohol was applied as a solvent, after pelleting with a 20-mesh sieve, 2.5% of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a honeycomb shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus.
- In the present example, 95 wt % of ferric oxalate was applied and 2.5 wt % of hydroxy methyl propyl cellulose was applied as an adhesive, and other coating processing etc. was the same as that in the first example.
- In the present example, 85 wt % of nickel citrate and 10 wt % of triethylamine hydrochlorate were applied, and other coating processing etc. was the same as that in the first example.
- In the present example, 95 wt % of nickel citrate was applied as a coolant, 2.5 wt % of hydroxymethyl propyl cellulose was added as an adhesive, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a bar shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus.
- The major difference from the first example is that 65 wt % of cobalt salicylate and 20 wt % of cobalt acetate were used and diethylamine hydrochloride in a mass percentage of 10% was used as an auxiliary fire extinguishing agent; other adhesive, release agent, content thereof and composition preparation etc. were the same as the first example.
- In the present example, 65 wt % of cobalt salicylate and 30 wt % of cobalt acetate were used, 2.5 wt % of hydroxy methyl propyl cellulose was added as an adhesive, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a tablet shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus.
- After preparing and shaping 50 g of the fire extinguishing compositions of the first example to the sixth example in tests, the fire extinguishing compositions were loaded to a fire extinguishing apparatus containing 50 g of a K-type aerosol generator, and 8B fire extinguishing tests were carried out on 3 fires in each group; specific test methods, test models and evaluation methods are as follows, and results are recorded in Table 1:
- test model: the oil disk is a GA86-2009 8B circular disk (diameter 570 mm, internal depth 150 mm and approximate area 0.25 m2);
- test method: 500 mm of water was added to the oil disk, then 2 mm of 93190 gasoline was added, the oil disk was pre-burning for 1 min and then began fire extinguishment;
- evaluation standard: it is considered that fire extinguishment is successful if there is no after-combustion 1 min after flame extinction and there is still gasoline remaining in the oil disk.
- A fire extinguishing test was performed for a fire extinguishing apparatus sample containing 100 g of a commercially available K-type hot aerosol fire extinguishing agent according to the same experiment model and experiment method as those in the examples above, and test results are as shown in Table 1.
-
TABLE 1 Test records of fire extinguishing compositions containing a salt of an organic acid of elements of group VIII Ingredient content of examples (mass percentage) Comparison Ingredient 1 2 3 4 5 6 1 K type agent • • • • • • • Ferric oxalate 75 95 — — Cobalt salicylate 65 65 Cobalt acetate 20 30 Nickel citrate 85 95 Diethylamine 20 10 hydrochloride Triethylamine 10 hydrochloride Hydroxy methyl 2.5 2.5 2.5 2.5 2.5 2.5 propyl cellulose Magnesium 2.5 2.5 2.5 2.5 2.5 2.5 stearate Fire extinguishing 6.2 7.0 6.0 6.0 6.0 6.2 time(s) Fire extinguishing 2 extinguished 1 extinguished 2 extinguished 1 extinguished All 1 extinguished Not situation in 3 in 3 in 3 in 3 extinguished in 3 extinguished - It can be clearly seen from Table 1 that the fire extinguishing compositions containing a salt of an organic acid of the fourth period transition metals in group VIII can meet basic fire extinguishing requirements of national standard GA86-2009 and there are no naked flames at all nozzles; the fire extinguishing performance is obviously better than that of the first comparison example and the fire extinguishing time is short.
- In the present example, 90 wt % of manganese acetate, 5 wt % of methacrylamide and 2.5 wt % of hydroxy methyl propyl cellulose were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- In the present example, 95 wt % of manganese acetate and 2.5 wt % of hydroxy methyl propyl cellulose were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- In the present example, 78 wt % of copper tartrate, 17 wt % of N,N′-methylenebisacrylamide and 2.5 wt % of hydroxy methyl propyl cellulose were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- In the present example, 95 wt % of copper tartrate, and 2.5 wt % of hydroxymethyl propyl cellulose were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- In the present example, 87 wt % of zinc acetate, 8 wt % of methacrylamide and 2.5 wt % of hydroxy methyl propyl cellulose were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- In the present example, 95 wt % of zinc acetate, and 2.5 wt % of hydroxy methyl propyl cellulose were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- In the present example, 60 wt % of manganese acetate, 35 wt % of cupric acetate and 2.5 wt % of hydroxymethyl propyl cellulose were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- In the present example, 94.7 wt % of manganese acetate, and 5.3 wt % of methacrylamide were mixed, industrial alcohol was used as a solvent, after pelleting with a 20-mesh sieve, 2.5 wt % of magnesium stearate was added as a release agent, all the above materials were mixed uniformly and then passed through a 15-mesh sieve, and shaped into a ball shape by using processes including pelleting, mould pressing and extruding etc. and loaded to a fire extinguishing apparatus containing 50 g of a K-type hot aerosol generator, a 93# gasoline fire extinguishing test of an oil disk having an area of 0.25 m2 was carried out; test results are as shown in Table 2 of test records.
- A 93# gasoline fire extinguishing test was performed on an oil disk having an area of 0.25 m2 for a fire extinguishing apparatus sample containing 100 g of a commercially available K-type hot aerosol fire extinguishing agent, and test results are as shown in Table 2.
-
TABLE 2 Test records of fire extinguishing compositions containing a salt of an organic acid of elements of a subgroup Ingredient content of examples (mass percentage) Comparison Ingredient 7 8 9 10 11 12 13 14 2 K type agent • • • • • • • • • Manganese acetate 90 95 60 94.7 Copper acetate 35 Copper tartrate 78 95 Zinc acetate 87 95 Methacrylamide 5 8 5.3 N,N′-methylene- 17 bisacrylamide Hydroxy methyl 2.5 2.5 2.5 2.5 2.5 2.5 2.5 2.5 propyl cellulose Magnesium stearate 2.5 2.5 2.5 2.5 2.5 2.5 2.5 2.5 Fire extinguishing 4.0 4.0 5.0 5.0 5.0 6.0 5.0 5.0 time(s) Fire extinguishing All All All 2 extiguished All All All All Not situation extinguished extinguished extinguished in 3 extinguished extinguished extinguished extinguished extinguished - It can be clearly seen from Table 2 that the fire extinguishing compositions containing an organic salt of transition metals in the group IB, the group IIB, and the group VIIB can completely meet basic fire extinguishing requirements of national standard GA86-2009 and there are no naked flames at all nozzles; the fire extinguishing performance is obviously better than that of the second comparison example and the fire extinguishing time is short. The fire extinguishing compositions containing an organic salt compound of transition metals in the group IB, the group IIB, and the group VIIB can meet ideal fire extinguishing requirements without addition of an auxiliary fire extinguishing ingredient in a certain mass percentage. However, by comprehensively considering aspects including spraying time, fire extinguishing time, the size of nozzle gas flows, spraying stability and processing etc.; a certain amount of an auxiliary fire extinguishing ingredient is added optimally.
Claims (17)
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| Application Number | Priority Date | Filing Date | Title |
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| CN201110451465 | 2011-11-20 | ||
| CN201110451465.5 | 2011-11-20 | ||
| CN201110451465.5A CN103170083B (en) | 2011-11-20 | 2011-12-20 | A fire extinguishing composition containing a transition metal compound |
| PCT/CN2012/080266 WO2013071782A1 (en) | 2011-11-20 | 2012-08-16 | Fire extinguishing composition containing transition metal compound |
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| US9717939B2 US9717939B2 (en) | 2017-08-01 |
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| US (1) | US9717939B2 (en) |
| EP (1) | EP2799118B1 (en) |
| CN (1) | CN103170083B (en) |
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| CN104190040B (en) * | 2014-09-09 | 2018-07-10 | 西安新竹防灾救生设备有限公司 | A kind of ABC ultra-fine dry powder extinguishing agents and preparation method thereof |
| CN110404225B (en) * | 2019-08-26 | 2022-02-15 | 西安科技大学 | An environmentally friendly polymer colloid fire extinguishing additive and its preparation method and application |
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Also Published As
| Publication number | Publication date |
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| WO2013071782A1 (en) | 2013-05-23 |
| MY198909A (en) | 2023-10-02 |
| EP2799118A1 (en) | 2014-11-05 |
| CN103170083A (en) | 2013-06-26 |
| CN103170083B (en) | 2016-04-06 |
| US9717939B2 (en) | 2017-08-01 |
| EP2799118A4 (en) | 2015-10-14 |
| EP2799118B1 (en) | 2019-07-10 |
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